Human Molecular Genetics, 2001, Vol. 10, No. 26 3101-3109
© 2001 Oxford University Press
Effect of allelic variation at the NACPRep1 repeat upstream of the
-synuclein gene (SNCA) on transcription in a cell culture luciferase reporter system
Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 49 Convent Drive, MSC 4472, Bethesda, MD 20892-4472, USA
Mutations in the
-synuclein gene (SNCA) have been implicated in familial Parkinsons disease (PD) while certain polymorphic alleles at a microsatellite repeat, NACPRep1, located
10 kb upstream of the gene, have been associated with sporadic PD. In order to study the regulation of the human
-synuclein gene, we performed a deletion analysis of 10.7 kb upstream of the translational start site, using the luciferase reporter assay in 293T cells and the neuroblastoma cell line SH-SY5Y. The shortest fragment, 400 bp upstream of the transcriptional start site, was sufficient for transcription in both cell lines. The other constructs led to variable expression levels, with some showing maximum expression and others showing nearly complete extinction of expression. An 880 bp fragment located
10 kb upstream of the gene and containing the NACPRep1 polymorphism, was shown to be necessary for normal expression. Additional analysis of the NACPRep1 locus and surrounding DNA suggested that two domains flanking the repeat interact to enhance expression while the repeat acts as a negative modulator. Next, we measured the activity of the entire 10.7 kb upstream region in the luciferase reporter assay when each of our different NACPRep1 alleles were present. The expression levels varied very significantly among the different alleles over a 3-fold range in the SH-SY5Y cells but showed little or no significant variation in the 293T cells. Given that even small changes in
-synuclein expression may, over many decades, predispose to PD, the association of different NACPRep1 alleles with PD may be a consequence of polymorphic differences in transcriptional regulation of
-synuclein expression resulting from different NACPRep1 alleles.
+ To whom correspondence should be addressed. Tel: +1 301 402 2039; Fax: +1 301 402 2170; Email: rlnuss@nhgri.nih.gov
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